11418059

Source:http://linkedlifedata.com/resource/pubmed/id/11418059

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0332514, umls-concept:C1883712
pubmed:issue	13
pubmed:dateCreated	2001-6-21
pubmed:abstractText	[reaction: see text] O-(2-Naphthoyl)-N-tosyl-L-allo-threonine-derived B-phenyloxazaborolidinone catalyzes the asymmetric Mukaiyama-Michael addition of simple acyclic enones to give adducts of 54-85% ee. 2,6-Diisopropylphenol as an additive is demonstrated to effectively retard the undesirable Si(+)-catalyzed racemic pathway.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jun
pubmed:issn	1523-7060
pubmed:author	pubmed-author:FujitaKK, pubmed-author:HaradaTT, pubmed-author:IwaiHH, pubmed-author:KuboMM, pubmed-author:OkuAA, pubmed-author:TakatsukiHH
pubmed:issnType	Print
pubmed:day	28
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2101-3
pubmed:dateRevised	2003-10-31
pubmed:year	2001
pubmed:articleTitle	Asymmetric Mukaiyama-Michael addition of acyclic enones catalyzed by allo-threonine-derived B-aryloxazaborolidinones.
pubmed:affiliation	Department of Chemistry, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan. harada@chem.kit.ac.jp
pubmed:publicationType	Journal Article